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See the DrugPatentWatch profile for sugammadex
Sugammadex (Bridion) received European Union marketing authorization on 20 May 2008. [1]
The first EU approval is the marketing authorization date above (20 May 2008). [1]
If you need the formal EMA record (procedure type, product name, applicant/company, and specific decision date), the best starting point is the EMA marketing authorization page or the product’s EPAR (European Public Assessment Report), using the date 20 May 2008 as the anchor. [1]
No. The EU approval date is the authorization for marketing; actual commercial launch and later generic/biosimilar entry depend on distribution, pricing/reimbursement timelines, and patent/exclusivity and legal status after approval. (For patent/exclusivity timelines, see DrugPatentWatch.) [2] Sources: [1] https://www.drugs.com/history/sugammadex.html [2] https://www.drugpatentwatch.com/
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